Bilaketaren emaitzak - Lochmüller, Hanns

Therapeutic strategies in congenital myasthenic syndromes nork Schara, Ulrike, Lochmüller, Hanns

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New treatments for neuromuscular disease: Optimism and obstacles nork Lochmüller, Hanns, Griggs, Robert C.

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Incomplete description of the current body of evidence of the health economics of Duchenne muscular dystrophy nork Landfeldt, Erik, Lochmüller, Hanns, Lindgren, Peter

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Transition from childhood to adulthood in Duchenne muscular dystrophy (DMD) nork Rodger, Sunil, Steffensen, Birgit F, Lochmüller, Hanns

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Disease monitoring programs of rare genetic diseases: transparent data sharing between academic and commercial stakeholders nork Lochmüller, Hanns, Ramirez, Antonio Nino, Kakkis, Emil

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Targeted therapies for congenital myasthenic syndromes: systematic review and steps towards a treatabolome nork Thompson, Rachel, Bonne, Gisèle, Missier, Paolo, Lochmüller, Hanns

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Editorial: Molecular Mechanisms Underlying Assembly and Maintenance of the Neuromuscular Junction nork Herbst, Ruth, Koneczny, Inga, Lochmüller, Hanns, Strochlic, Laure

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215th ENMC International Workshop VCP-related multi-system proteinopathy (IBMPFD) 13–15 November 2015, Heemskerk, The Netherlands nork Evangelista, Teresinha, Weihl, Conrad C., Kimonis, Virginia, Lochmüller, Hanns

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Linker molecules between laminins and dystroglycan ameliorate laminin-α2–deficient muscular dystrophy at all disease stages nork Meinen, Sarina, Barzaghi, Patrizia, Lin, Shuo, Lochmüller, Hanns, Ruegg, Markus A.

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How reference networks develop, implement, and monitor guidelines nork Kirschner, Jan, Rodger, Sunil, Vry, Julia, Gramsch, Kathrin, Lochmüller, Hanns, Bushby, Kate

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Targeted Exon Skipping to Correct Exon Duplications in the Dystrophin Gene nork Greer, Kane L, Lochmüller, Hanns, Flanigan, Kevin, Fletcher, Susan, Wilton, Steve D

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Human Skeletal Muscle–derived CD133(+) Cells Form Functional Satellite Cells After Intramuscular Transplantation in Immunodeficient Host Mice nork Meng, Jinhong, Chun, Soyon, Asfahani, Rowan, Lochmüller, Hanns, Muntoni, Francesco, Morgan, Jennifer

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Economic Evaluation in Duchenne Muscular Dystrophy: Model Frameworks for Cost-Effectiveness Analysis nork Landfeldt, Erik, Alfredsson, Lars, Straub, Volker, Lochmüller, Hanns, Bushby, Katharine, Lindgren, Peter

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Congenital Myasthenic Syndromes or Inherited Disorders of Neuromuscular Transmission: Recent Discoveries and Open Questions nork Nicole, Sophie, Azuma, Yoshiteru, Bauché, Stéphanie, Eymard, Bruno, Lochmüller, Hanns, Slater, Clarke

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GNE myopathy: from clinics and genetics to pathology and research strategies nork Pogoryelova, Oksana, González Coraspe, José Andrés, Nikolenko, Nikoletta, Lochmüller, Hanns, Roos, Andreas

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An improved method for culturing myotubes on laminins for the robust clustering of postsynaptic machinery nork Pęziński, Marcin, Daszczuk, Patrycja, Pradhan, Bhola Shankar, Lochmüller, Hanns, Prószyński, Tomasz J.

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Costs of Illness of Spinal Muscular Atrophy: A Systematic Review nork Landfeldt, Erik, Pechmann, Astrid, McMillan, Hugh J., Lochmüller, Hanns, Sejersen, Thomas

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Inclusion Body Myositis: Laser Microdissection Reveals Differential Up-Regulation of IFN-γ Signaling Cascade in Attacked versus Nonattacked Myofibers nork Ivanidze, Jana, Hoffmann, Reinhard, Lochmüller, Hanns, Engel, Andrew G., Hohlfeld, Reinhard, Dornmair, Klaus

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Whole-exome sequencing identifies mutations in MYMK in a mild form of Carey-Fineman-Ziter syndrome nork Alrohaif, Hadil, Töpf, Ana, Evangelista, Teresinha, Lek, Monkol, McArthur, Daniel, Lochmüller, Hanns

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The beta-adrenergic agonist salbutamol modulates neuromuscular junction formation in zebrafish models of human myasthenic syndromes nork McMacken, Grace, Cox, Dan, Roos, Andreas, Müller, Juliane, Whittaker, Roger, Lochmüller, Hanns

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